Bloemendal A, Van der Zee R, Rutten V P, van Kooten P J, Farine J C, van Eden W
Institute of Infectious Diseases and Immunology, Utrecht University, The Netherlands.
Clin Exp Immunol. 1997 Oct;110(1):72-8. doi: 10.1046/j.1365-2249.1997.4841378.x.
OM-89 is a bacterial (Escherichia coli) extract used for oral administration in the treatment of RA. Given the evidence that immunity to bacterial heat shock antigens plays a critical role in the immunomodulation of arthritis and possibly inflammation in general, the purpose of the present studies was to evaluate the presence and immunogenicity of hsp in OM-89. Furthermore, we studied the effects of OM-89 in an experimental arthritis, where hsp are known to have a critical significance in disease development. In rats immunization with OM-89 was found to lead to proliferative T cell responses to hsp60 and hsp70 of both E. coli and mycobacterial origin. Conversely, immunization with hsp antigens was also found to induce T cell reactivity specific for OM-89. Based on this and the antigen specificity analysis of specific T cell lines, hsp70(DnaK) turned out to be one of the major immunogenic constituents of OM-89. Parenteral immunization with OM-89 was found to reduce resistance to adjuvant arthritis (AA), whereas oral administration was found to protect against AA. Given the arthritis-inhibitory effect of oral OM-89 in AA, it is possible that peripheral tolerance is induced at the level of regulatory T cells with specificity for hsp. This may also constitute a mode of action for OM-89 as an arthritis-suppressive oral drug.
OM-89是一种用于口服治疗类风湿性关节炎(RA)的细菌(大肠杆菌)提取物。鉴于有证据表明对细菌热休克抗原的免疫在关节炎的免疫调节以及可能在一般炎症中起关键作用,本研究的目的是评估OM-89中热休克蛋白(hsp)的存在情况及其免疫原性。此外,我们研究了OM-89在实验性关节炎中的作用,已知hsp在该疾病发展中具有关键意义。在大鼠中,发现用OM-89免疫会导致对大肠杆菌和分枝杆菌来源的hsp60和hsp70产生增殖性T细胞反应。相反,用hsp抗原免疫也被发现会诱导对OM-89具有特异性的T细胞反应性。基于此以及对特定T细胞系的抗原特异性分析,hsp70(DnaK)被证明是OM-89的主要免疫原性成分之一。发现用OM-89进行肠胃外免疫会降低对佐剂性关节炎(AA)的抵抗力,而口服则被发现可预防AA。鉴于口服OM-89对AA具有关节炎抑制作用,有可能在对hsp具有特异性的调节性T细胞水平上诱导外周耐受。这也可能构成OM-89作为一种抑制关节炎的口服药物的作用方式。